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(2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid

Base Information
  • Chemical Name:(2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid
  • CAS No.:1167421-25-1
  • Molecular Formula:C9H17N5O4
  • Molecular Weight:259.26238
  • Hs Code.:
(2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid

Synonyms:(2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid

Suppliers and Price of (2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Nε-2-Azidoethyloxycarbonyl-L-lysine
  • 100mg
  • $ 150.00
Total 35 raw suppliers
Chemical Property of (2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid
Chemical Property:
  • PSA:151.40000 
  • LogP:1.14906 
Purity/Quality:

99% ,98%,Electron Grade , *data from raw suppliers

Nε-2-Azidoethyloxycarbonyl-L-lysine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Nε-2-Azidoethyloxycarbonyl-L-lysine is derived from 2-Azidoethanol (A848560), which is used as a reagent in the glycosylation of mono- or polysaccharides. 2-Azidoethanol is also used as a 2’-deoxy-ethynyluridine (EdU) blocker in nuclear DNA, preventing cross relativity with other antibodies in order to better study its related pathways in the body.
Technology Process of (2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid

There total 8 articles about (2S)-2-amino-6-{[(2-azidoethoxy)carbonyl]amino}hexanoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; water; In 1,4-dioxane; at 5 - 47 ℃; for 5h; Temperature; Inert atmosphere;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium azide / N,N-dimethyl-formamide / 48 h / 70 °C
2: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C
With sodium azide; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja210587q
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